Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
In this study, PP-001 eye drops are assessed for safety and tolerability in healthy, adult volunteers. PP-001 is a novel, anti-inflammatory small molecule that inhibits a specific enzyme (Dihydroorotate Dehydrogenase).
The study was amended and now includes patients with ocular surface inflammation.
In this prospective, single-centre, double blind (within each cohort), placebo controlled, randomised study, safety and tolerability of PP-001 eye drops is assessed in healthy, adult volunteers (cohorts 1-3) and in patients with ocular surface inflammation (cohort 4). PP-001 is a novel small molecule inhibitor of Dihydroorotate Dehydrogenase (DHODH) with anti-inflammatory properties.
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| PP-001 verum - cohort 1 | Experimental | PP-001 verum - cohort 1 |
|
| Placebo - cohort 1 | Placebo Comparator | Placebo - cohort 1 |
|
| PP-001 verum - cohort 2 | Experimental | PP-001 verum - cohort 2 |
|
| Placebo - cohort 2 | Placebo Comparator | Placebo - cohort 2 |
|
| PP-001 verum - cohort 3 | Experimental | PP-001 verum - cohort 3 |
|
| Placebo - cohort 3 | Placebo Comparator | Placebo - cohort 3 |
|
| PP-001 verum - cohort 4 |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| PP-001 | Drug | PP-001 eye drops |
|
| Measure | Description | Time Frame |
|---|---|---|
| Evaluation of safety and tolerability by determining treatment emergent adverse events | To assess safety and tolerability of ascending, multiple daily doses of PP-001 eye drops in healthy, adult volunteers and in patients with ocular surface inflammation | 28 days (cohorts 1-3) and 20 days (cohort 4) |
| Measure | Description | Time Frame |
|---|---|---|
| Evaluation of Peak Plasma Concentration (Cmax) in peripheral blood | To evaluate the pharmacokinetics (Cmax) of PP-001 in healthy, adult volunteers following single and multiple daily ocular instillation | 1 and 12 days (cohorts 1-3) |
| Evaluation of area under the plasma concentration versus time curve (AUC) in peripheral blood |
Not provided
Inclusion Criteria (excerpt):
Cohorts 1-3:
Cohort 4:
Exclusion Criteria (excerpt):
Cohorts 1-4:
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University Hospital Vienna | Vienna | Austria |
Not provided
| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot | Yes | No | No | Study Protocol | Mar 26, 2021 | Jan 2, 2024 | Prot_000.pdf |
| SAP | No | Yes | No | Statistical Analysis Plan | Oct 12, 2021 | Jan 2, 2024 | SAP_001.pdf |
Not provided
| ID | Term |
|---|---|
| D007637 | Keratoconjunctivitis |
| ID | Term |
|---|---|
| D003231 | Conjunctivitis |
| D003229 | Conjunctival Diseases |
| D005128 | Eye Diseases |
| D007634 | Keratitis |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Experimental |
PP-001 verum - cohort 4 |
|
| Placebo - cohort 4 | Placebo Comparator | Placebo - cohort 4 |
|
| Placebo | Other | Placebo eye drops |
|
To evaluate the pharmacokinetics (AUC) of PP-001 in healthy, adult volunteers following single and multiple daily ocular instillation |
| 1 and 12 days (cohorts 1-3) |
| D003316 |
| Corneal Diseases |